संक्रामक रोग और पैथोलॉजी जर्नल

खुला एक्सेस

हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।

ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं

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अमूर्त

In the Aged Stomach, Gastric Repair Does Not Lead to the Development of Spasmolytic Polypeptide/TFF2-Expressing Metaplasia

Yana Zavros

Background & Aims: During aging, physiological changes in the stomach result in further tenuous gastric towel that's lower able of repairing injury, leading to increased vulnerability to habitual ulceration. Spasmolytic polypeptide/ trefoil factor 2 – expressing metaplasia (SPEM) is known to crop after parietal cell loss and during Helicobacter pylori infection; still, its part in gastric ulcer form is unknown. Thus, we sought to probe if SPEM plays a part in epithelial rejuvenescence.

Methods: Acetic acid ulcers were convinced in youthful (2 – 3 mo) and aged (18 – 24 mo) C57BL/ 6 mice to determine the quality of ulcer form with advancing age. Unheroic trimmer3.0 mice were used to induce unheroic fluorescent protein – expressing organoids for transplantation. Unheroic fluorescent protein – positive gastric organoids were scattered into the sub mucosa and lumen of the stomach incontinently after ulcer induction. Gastric towel was collected and anatomized to determine the engraftment of organoid- deduced cells within the regenerating epithelium.

Results: Crack mending in youthful mice coincided with the emergence of SPEM within the ulcerated region, a response that was absent in the aged stomach. Although aged mice showed lower metaplasia girding the ulcerated towel, organoid- transplanted aged mice showed regenerated gastric glands containing organoid- deduced cells. Organoid transplantation in the aged mice led to the emergence of SPEM and gastric rejuvenescence.

Conclusion: These data show the development of SPEM during gastric form in response to injury that's absent in the aged stomach. In addition, gastric organoid in an injury/ transplantation mouse model promoted gastric rejuvenescence.